4.6 Article

An enzyme-free fluorescent sensing platform for the detection of uric acid in human urine

Journal

JOURNAL OF LUMINESCENCE
Volume 236, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.jlumin.2021.118076

Keywords

Lanthanide metal-organic framework; Electrospinning fiber membrane; Enzyme-free; Fluorescent sensing platform; Uric acid

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Funding

  1. National Natural Science Foundation of China [82073811, 81673394]
  2. Fundamental Research Funds for the Central Universities [2042020kf1010]

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An efficient uric acid detection method was developed using an enzyme-free fluorescent sensing platform based on lanthanide metal-organic framework-doped electrospinning fiber membrane. The method showed excellent fluorescence performance and accurate detection of uric acid concentration in urine samples.
An enzyme-free fluorescent sensing platform based on lanthanide metal-organic framework (Eu-BDC, BDC:1,4-benzenedicarboxylic acid) doped electrospinning fiber membrane (Eu-BDC@FM) was established for the detection of uric acid (UA) in human urine. The Eu-BDC@FM has Eu3+ characteristic emission, excellent fluorescence stability in pH 4.5-8.0, appropriate hydrophilicity and good reusability (at least 5 cycles). The fluorescence intensity of Eu-BDC@FM can be quenched by UA through inner filter effect. The relationship between the quenching efficiency and UA concentration [A] accords with Stern-Volmer formula in the range of 0-200 mu M: I-0/I = 0.0106 [A]+1.0199 (r = 0.9933), where I-0 and I are the fluorescence intensity of Eu-BDC@FM immersed in water and the UA aqueous solution respectively. The quenching constant is 10.6 x 10(3) M-1 and the limit of detection is 0.6 mu M. The Eu-BDC@FM-based fluorescent sensing platform was applied to detect UA in real urine samples. The common substances in human urine have no interference with UA sensing, and the recovery is in the range of 95-110% with relative standard deviation less than 2.0%. The proposed method is simple, robust, inexpensive, and has good selectivity, accuracy and precision for quantification of UA in real urine samples.

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